Device recall
Z-1741-2017: Covidien Curity Eye Pad Item Code: 91650 The sterile eye pad is a device that…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-1741-2017 |
|---|---|
| Recall event | 76606 |
| Product | Covidien Curity Eye Pad Item Code: 91650 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions. It is supplied sterile to allow for use in the operating room… |
| Product code | HMP |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2019 |
| FEI number | 1219930 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database